Original scientific paper
https://doi.org/10.15255/KUI.2024.025
Computational Modelling of Anti-Carcinogenic Effects of Naringenin
Lamija Ahmetović
orcid.org/0009-0009-4172-3356
; University of Maribor, Faculty of Chemistry and Chemical Engineering, Smetanova 17, SI-2000 Maribor, Slovenia
Veronika Furlan
; University of Maribor, Faculty of Chemistry and Chemical Engineering, Smetanova 17, SI-2000 Maribor, Slovenia
Urban Bren
; University of Maribor, Faculty of Chemistry and Chemical Engineering, Smetanova 17, SI-2000 Maribor, Slovenia
*
* Corresponding author.
Abstract
Naringenin is a bioactive polyphenol derived from citrus fruits, known for its various beneficial effects on human health. This study focuses on naringenin as a polyphenolic scavenger of nine ultimate chemical carcinogens: 2-cyanoethylene oxide, aflatoxin B1 exo-8,9-epoxide, glycidamide, ethylene oxide, propylene oxide, styrene oxide, vinyl carbamate epoxide, chloroethylene oxide, and β-propiolactone. The aim was to calculate the activation free energies and elucidate the molecular mechanisms of alkylation reactions between naringenin and these genotoxic chemical carcinogens, using the quantum-mechanical Hartree-Fock method in combination with two flexible basis sets, 6-31G(d) and 6-311++G(d,p). Activation free energy calculations were performed using Gaussian 09 in a vacuum and with two implicit solvation models: Polarisable Continuum Model and Langevin Dipoles. To assess naringenin’s scavenging efficacy, the activation free energies calculated using these solvation models, were compared to the experimental values of the activation free energies between the same ultimate chemical carcinogens and the most reactive DNA base, guanine.
The findings indicated naringenin's efficacy as a polyphenolic scavenger of six ultimate chemical carcinogens, particularly β-propiolactone, vinyl carbamate epoxide, and propylene oxide. For chloroethylene oxide, aflatoxin B1 exo-8,9-epoxide, and ethylene oxide, naringenin also demonstrated significant anti-carcinogenic potential, as the calculated activation free energies were comparable to experimentally determined values for guanine. However, naringenin's protective activity was less potent against 2-cyanoethylene oxide, glycidamide, and styrene oxide, where the calculated activation free energies were significantly higher than the experimental values for guanine.
Keywords
naringenin; ultimate chemical carcinogens; activation free energies; Hartree-Fock method; implicit solvation models
Hrčak ID:
322991
URI
Publication date:
12.12.2024.
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